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Updated: Jan 11, 2026

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
Published on: February 6, 2020
Exploring transamidation and chemical recycling of β-amino amide-derived covalent adaptable networks
Loc Tan Nguyen1, Adithya Tharayil1, Nezha Badi1
1Polymer Chemistry Research Group, Centre of Macromolecular Chemistry (CMaC), Department of Organic and Macromolecular Chemistry, Faculty of Sciences, Ghent University Krijgslaan 291 S4 9000 Ghent Belgium Filip.DuPrez@UGent.be.
Abstract:
The growing environmental challenge of non-recyclable thermosets underscores the urgent need for sustainable alternatives. Covalent adaptable networks (CANs) containing dynamic β-amino amide moieties have emerged as promising reprocessable polymer networks, combining mechanical robustness with recyclability. In this work, we elucidate the exchange kinetics of both the well-established (retro)-aza-Michael addition and a newly identified transamidation pathway that is operative in β-amino amides. Systematic catalyst screening reveals that acidic catalysts significantly enhance viscoelastic control, thereby improving (re)processing efficiency. Furthermore, we introduce a chemical recycling protocol that enables the recovery of the original amino building blocks with up to 86% purity, demonstrating their direct use as feedstock in material (re)synthesis. These insights advance the fundamental understanding of dynamic bond exchange in β-amino amide based CANs and establish a viable route towards circular thermoset materials for numerous applications.
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